DB1976 |
| Catalog No.GC39627 |
DB1976은 DB270의 셀레노펜 유사체이며 강력하고 세포 투과성이 있으며 완전히 효과적인 전사 인자 PU.1 억제제입니다. DB1976은 시험관 내에서 PU.1 결합(IC50 10nM)을 강력하게 억제하고 PU.1/DNA 복합체(높은 DB1976-ΛB 친화성, KD 12nM)를 강력하게 억제합니다. DB1976은 세포사멸을 유도하는 효과가 있습니다.
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Cas No.: 1557397-51-9
Sample solution is provided at 25 µL, 10mM.
DB1976 is a selenophene analog of DB270 and a potent and cell-permeable fully efficacious transcription factor PU.1 inhibitor. DB1976 potently inhibits PU.1 binding (IC50 of 10 nM) and strongly inhibits the PU.1/DNA complex (with high DB1976-ΛB affinity, KD of 12 nM) in vitro. DB1976 has apoptosis-inducing effect[1][2][3].
[1]. Munde M, et al. Structure-dependent inhibition of the ETS-family transcription factor PU.1 by novel heterocyclic diamidines. Nucleic Acids Res. 2014 Jan;42(2):1379-90. [2]. Stephens DC, et al. Pharmacologic efficacy of PU.1 inhibition by heterocyclic dications: a mechanistic analysis. Nucleic Acids Res. 2016 May 19;44(9):4005-13. [3]. Antony-DebrÉ I, et al. Pharmacological inhibition of the transcription factor PU.1 in leukemia. J Clin Invest. 2017 Dec 1;127(12):4297-4313.
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